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WO2008033749A3 - Inhibiteurs d'egfr à base de quinazoline contenant un fragment de liaison au zinc - Google Patents

Inhibiteurs d'egfr à base de quinazoline contenant un fragment de liaison au zinc Download PDF

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Publication number
WO2008033749A3
WO2008033749A3 PCT/US2007/077977 US2007077977W WO2008033749A3 WO 2008033749 A3 WO2008033749 A3 WO 2008033749A3 US 2007077977 W US2007077977 W US 2007077977W WO 2008033749 A3 WO2008033749 A3 WO 2008033749A3
Authority
WO
WIPO (PCT)
Prior art keywords
binding moiety
egfr inhibitors
zinc binding
inhibitors containing
based egfr
Prior art date
Application number
PCT/US2007/077977
Other languages
English (en)
Other versions
WO2008033749A2 (fr
Inventor
Changgeng Qian
Xiong Cai
Stephen Gould
Haixiao Zhai
Original Assignee
Curis Inc
Changgeng Qian
Xiong Cai
Stephen Gould
Haixiao Zhai
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Curis Inc, Changgeng Qian, Xiong Cai, Stephen Gould, Haixiao Zhai filed Critical Curis Inc
Priority to AU2007296746A priority Critical patent/AU2007296746B2/en
Priority to EP07842116A priority patent/EP2061773A4/fr
Priority to BRPI0715016-4A priority patent/BRPI0715016A2/pt
Priority to KR1020137002341A priority patent/KR101434164B1/ko
Priority to MX2009002585A priority patent/MX2009002585A/es
Priority to CN200780041896.6A priority patent/CN101535279B/zh
Priority to JP2009527603A priority patent/JP5580592B2/ja
Priority to CA2662617A priority patent/CA2662617C/fr
Publication of WO2008033749A2 publication Critical patent/WO2008033749A2/fr
Publication of WO2008033749A3 publication Critical patent/WO2008033749A3/fr
Priority to IL197451A priority patent/IL197451A/en

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/70—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
    • C07D239/72—Quinazolines; Hydrogenated quinazolines
    • C07D239/86—Quinazolines; Hydrogenated quinazolines with hetero atoms directly attached in position 4
    • C07D239/88—Oxygen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/70—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
    • C07D239/72—Quinazolines; Hydrogenated quinazolines
    • C07D239/86—Quinazolines; Hydrogenated quinazolines with hetero atoms directly attached in position 4
    • C07D239/94—Nitrogen atoms
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/517—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with carbocyclic ring systems, e.g. quinazoline, perimidine
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A61P35/02—Antineoplastic agents specific for leukemia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A61P35/04—Antineoplastic agents specific for metastasis
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/70—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
    • C07D239/72—Quinazolines; Hydrogenated quinazolines
    • C07D239/86—Quinazolines; Hydrogenated quinazolines with hetero atoms directly attached in position 4
    • C07D239/93—Sulfur atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/04—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
    • C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oncology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Hematology (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

La présente invention concerne des dérivés à base de quinazoline contenant un fragment de liaison au zinc, qui présentent des propriétés améliorées et inattendues en tant qu'inhibiteurs de la tyrosine kinase du récepteur du facteur de croissance épidermique (EGFR-TK), ainsi que leur utilisation dans le traitement de maladies et de troubles associés à la EGFR-TK, notamment le cancer. Lesdits dérivés peuvent également faire office d'inhibiteurs d'HDAC.
PCT/US2007/077977 2006-09-11 2007-09-10 Inhibiteurs d'egfr à base de quinazoline contenant un fragment de liaison au zinc WO2008033749A2 (fr)

Priority Applications (9)

Application Number Priority Date Filing Date Title
AU2007296746A AU2007296746B2 (en) 2006-09-11 2007-09-10 Quinazoline based EGFR inhibitors containing a zinc binding moiety
EP07842116A EP2061773A4 (fr) 2006-09-11 2007-09-10 Inhibiteurs d'egfr à base de quinazoline contenant un fragment de liaison au zinc
BRPI0715016-4A BRPI0715016A2 (pt) 2006-09-11 2007-09-10 composiÇço, composiÇço farmacÊutica, mÉtodo para tratar uma doenÇa ou distérbio relacionada com tirosina quinase de egfr em um individuo necessitando o mesmo, mÉtodo para tratar uma doenÇa mediada por hdac e mÉtodo para tratar doenÇas medidas tanto por tirosina quinase de egfr quanto hdac
KR1020137002341A KR101434164B1 (ko) 2006-09-11 2007-09-10 아연 결합 부분을 함유한 퀴나졸린 계열 ｅｇｆｒ 억제제
MX2009002585A MX2009002585A (es) 2006-09-11 2007-09-10 Inhibidores e egfr a base de quinolina que contienen porcion de enlace de zinc.
CN200780041896.6A CN101535279B (zh) 2006-09-11 2007-09-10 含锌结合基的喹唑啉基egfr抑制剂
JP2009527603A JP5580592B2 (ja) 2006-09-11 2007-09-10 亜鉛結合部分を含むキナゾリン系ｅｇｆｒインヒビター
CA2662617A CA2662617C (fr) 2006-09-11 2007-09-10 Inhibiteurs d'egfr a base de quinazoline contenant un fragment de liaison au zinc
IL197451A IL197451A (en) 2006-09-11 2009-03-05 History of Phenylamino and 4-Phenylalkylamino Quinazoline and Pharmaceuticals Containing It

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US84364406P 2006-09-11 2006-09-11
US60/843,644 2006-09-11
US89587307P 2007-03-20 2007-03-20
US60/895,873 2007-03-20

Publications (2)

Publication Number Publication Date
WO2008033749A2 WO2008033749A2 (fr) 2008-03-20
WO2008033749A3 true WO2008033749A3 (fr) 2008-12-04

Family

ID=39184477

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US2007/077977 WO2008033749A2 (fr) 2006-09-11 2007-09-10 Inhibiteurs d'egfr à base de quinazoline contenant un fragment de liaison au zinc

Country Status (13)

Country Link
US (5) US8604044B2 (fr)
EP (1) EP2061773A4 (fr)
JP (1) JP5580592B2 (fr)
KR (2) KR101434164B1 (fr)
CN (1) CN101535279B (fr)
AU (1) AU2007296746B2 (fr)
BR (1) BRPI0715016A2 (fr)
CA (1) CA2662617C (fr)
IL (1) IL197451A (fr)
MX (1) MX2009002585A (fr)
SG (1) SG174774A1 (fr)
TW (2) TWI399204B (fr)
WO (1) WO2008033749A2 (fr)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8735409B2 (en) 2009-12-21 2014-05-27 Qiang Zhang Quinazoline derivatives
US9434994B2 (en) 2004-05-27 2016-09-06 The Regents Of The University Of Colorado, A Body Corporate Methods for prediction of clinical outcome to epidermal growth factor receptor inhibitors by non-small cell lung cancer patients
US11524956B2 (en) 2011-03-04 2022-12-13 Newgen Therapeutics, Inc. Alkyne substituted quinazoline compound and methods of use

Families Citing this family (55)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2005070020A2 (fr) 2004-01-23 2005-08-04 The Regents Of The University Of Colorado Expression genique relative a la sensibilite au gefitinib, produits et procedes associes
EP2061469B8 (fr) 2006-09-11 2014-02-26 Curis, Inc. Inhibiteurs d'egfr à base de quinazoline
US7547781B2 (en) * 2006-09-11 2009-06-16 Curis, Inc. Quinazoline based EGFR inhibitors containing a zinc binding moiety
SG174772A1 (en) * 2006-09-11 2011-10-28 Curis Inc Multi-functional small molecules as anti-proliferative agents
KR101434164B1 (ko) 2006-09-11 2014-08-26 쿠리스 인코퍼레이션 아연 결합 부분을 함유한 퀴나졸린 계열 ｅｇｆｒ 억제제
US8119616B2 (en) * 2007-09-10 2012-02-21 Curis, Inc. Formulation of quinazoline based EGFR inhibitors containing a zinc binding moiety
ES2526718T3 (es) * 2007-09-10 2015-01-14 Curis, Inc. Inhibidores de EGFR basados en sales de tartrato o complejos de quinazolina que contienen un resto que se une al cinc
US8252805B2 (en) 2008-05-07 2012-08-28 Teva Pharmaceutical Industries Ltd. Forms of lapatinib ditosylate and processes for preparation thereof
US20100197915A1 (en) * 2008-08-06 2010-08-05 Leonid Metsger Lapatinib intermediates
KR101430424B1 (ko) 2009-01-08 2014-08-14 쿠리스 인코퍼레이션 아연 결합 모이어티를 갖는 포스포이노시티드 ３-키나제 억제제
CN101899011B (zh) * 2009-05-26 2013-01-16 北京大学 氨基二硫代甲酸酯类化合物、其制备方法和应用
PE20121091A1 (es) 2009-10-22 2012-08-17 Gilead Sciences Inc Derivados de purina o deazapurina utiles en el tratamiento de (inter alia) infecciones virales
CN101857617A (zh) * 2010-04-28 2010-10-13 中国海洋大学 喹唑啉类糖衍生物及其制备方法和应用
CN102452988B (zh) * 2010-10-27 2016-01-27 中国科学院化学研究所 一种喹唑啉衍生物及其制备方法
MX341456B (es) 2011-03-04 2016-08-18 Glaxosmithkline Ip Dev Ltd Amino-quinolinas como inhibidores de cinasa.
WO2012125904A1 (fr) 2011-03-17 2012-09-20 The Trustees Of The University Of Pennsylvania Composés imitant des mutations qui se lient au domaine kinase de l'egfr
WO2012125913A1 (fr) 2011-03-17 2012-09-20 The Trustees Of The University Of Pennsylvania Procédés et utilisation de molécules en forme de pince générant une enzyme bifonctionnelle
EP3111938B1 (fr) 2011-04-01 2019-05-08 Curis, Inc. Inhibiteur de phosphoinositide3-kinase avec une fraction de liaison au zinc
CN102918029B (zh) * 2011-05-17 2015-06-17 江苏康缘药业股份有限公司 4-苯胺-6-丁烯酰胺-7-烷醚喹唑啉衍生物及其制备方法和用途
US9499530B2 (en) 2011-08-01 2016-11-22 Hangzhou Minsheng Institutes For Pharma Research Quinazoline derivative, composition having the derivative, and use of the derivative in preparing medicament
TWI547494B (zh) 2011-08-18 2016-09-01 葛蘭素史克智慧財產發展有限公司 作為激酶抑制劑之胺基喹唑啉類
CN102408411B (zh) * 2011-09-19 2014-10-22 北京康辰药业股份有限公司 一种含喹啉基的羟肟酸类化合物及其制备方法、以及含有该化合物的药物组合物及其应用
CN102659764A (zh) * 2012-04-16 2012-09-12 中国科学院广州生物医药与健康研究院 酪氨酸激酶不可逆抑制剂及其制备方法和用途
WO2013159698A1 (fr) * 2012-04-26 2013-10-31 深圳信立泰药业股份有限公司 Composé cyclique condensé de quinazoline-acide hydroximique et son utilisation comme médicament antitumoral
CN102659692B (zh) 2012-05-04 2014-04-09 郑州泰基鸿诺药物科技有限公司 双联厄洛替尼及其制备方法
CN104736155B (zh) * 2012-05-14 2018-01-02 杭州德润玉成生物科技有限公司 双环化合物作为激酶的抑制剂
AR092529A1 (es) 2012-09-13 2015-04-22 Glaxosmithkline Llc Compuesto de aminoquinazolina, composicion farmaceutica que lo comprende y uso de dicho compuesto para la preparacion de un medicamento
CN102898315B (zh) * 2012-11-05 2015-01-28 上海毕得医药科技有限公司 3-乙炔基-4-氟苯胺的制备方法
CN103896860B (zh) * 2012-12-25 2016-02-17 通化济达医药有限公司 含有锌结合基的不可逆egfr抑制剂
CN103965174B (zh) * 2013-02-01 2016-05-11 通化济达医药有限公司 含有锌结合基的喹唑啉基egfr酪氨酸激酶抑制剂
CN103965106A (zh) * 2013-02-01 2014-08-06 通化济达医药有限公司 含有锌结合基的喹啉基egfr酪氨酸激酶抑制剂
CN103965119B (zh) * 2013-02-02 2016-07-06 通化济达医药有限公司 含有锌结合基的不可逆egfr酪氨酸激酶抑制剂
ES2654100T3 (es) 2013-02-21 2018-02-12 Glaxosmithkline Intellectual Property Development Limited Quinazolinas como inhibidores de quinasa
US9840494B2 (en) 2013-12-12 2017-12-12 Tianjin Hemay Oncology Pharmaceutical Co., Ltd. Quinazoline derivative
CN104761507B (zh) * 2014-01-06 2019-11-12 广东东阳光药业有限公司 氨基喹唑啉衍生物及其在药物中的应用
WO2015154725A1 (fr) * 2014-04-11 2015-10-15 四川海思科制药有限公司 Dérivé quinazoline, et son procédé de préparation et son utilisation en médecine
JP6662917B2 (ja) * 2015-03-18 2020-03-11 グアンドン・チョンシェン・ファーマスーティカル・カンパニー・リミテッド ヒストン脱アセチル化酵素阻害剤、並びにその調製方法及び使用
US9890187B2 (en) 2015-06-26 2018-02-13 Epos-Iasis Research And Development, Ltd. Prototype systems of theranostic biomarkers for in vivo molecular management of cancer
CN105001167B (zh) * 2015-07-16 2018-01-05 西安交通大学 1‑取代苯基‑3‑（4‑取代苯基氨基‑6‑喹唑啉基）脲类化合物及制备方法和用途
US11171324B2 (en) 2016-03-15 2021-11-09 Honda Motor Co., Ltd. System and method of producing a composite product
CN106045923A (zh) * 2016-03-17 2016-10-26 广东众生药业股份有限公司 一种组蛋白去乙酰化酶抑制剂及其制备方法和用途
US20190322643A1 (en) * 2016-06-29 2019-10-24 Georgia State University Research Foundation, Inc. Histone deacetylase and histone methyltransferase inhibitors and methods of making and use of the same
US11395821B2 (en) 2017-01-30 2022-07-26 G1 Therapeutics, Inc. Treatment of EGFR-driven cancer with fewer side effects
CN108285421A (zh) * 2018-01-26 2018-07-17 黑龙江鑫创生物科技开发有限公司 一种微通道反应器合成拉帕替尼中间体的方法
CN110642796B (zh) * 2018-06-27 2023-03-17 烟台药物研究所 一种喹唑啉类衍生物及其应用
MX2021002805A (es) 2018-09-10 2021-07-15 Mirati Therapeutics Inc Terapias de combinacion.
MX2021002742A (es) 2018-09-11 2021-08-11 Curis Inc Terapia combinada con un inhibidor de la fosfoinositida 3-quinasa con un resto de unión a zinc.
AU2019346550A1 (en) 2018-09-25 2021-04-22 Black Diamond Therapeutics, Inc. Quinazoline derivatives as tyrosine kinase inhibitor, compositions, methods of making them and their use
CN110903253B (zh) * 2019-12-13 2020-12-25 西安交通大学医学院第一附属医院 一种喹唑啉酮类化合物及其制备方法和应用
US20240123072A1 (en) * 2021-01-20 2024-04-18 LightOx Limited Protected hdac (histone deacetylase) inhibitors
CN113444052A (zh) * 2021-07-01 2021-09-28 江苏君若药业有限公司 吉非替尼的合成
CN114685382B (zh) * 2022-04-14 2024-02-06 河北医科大学 具有HDACs抑制活性的喹唑啉-4-胺衍生物及其制备方法与用途
CN116444447B (zh) * 2023-06-19 2023-09-22 中国药科大学 一种sos1和hdac双靶点喹唑啉羟肟酸化合物及其制法和应用
CN118724907B (zh) * 2024-06-03 2025-10-03 北京化工大学 一种大环多胺衍生的喹唑啉化合物及其制备方法与应用
CN119431189A (zh) * 2024-08-06 2025-02-14 惠州市第一人民医院 羟肟酸化合物及其应用

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5616582A (en) * 1992-01-20 1997-04-01 Zeneca Limited Quinazoline derivatives as anti-proliferative agents
US5942514A (en) * 1995-04-27 1999-08-24 Zeneca Limited Quinazoline derivatives
US6184225B1 (en) * 1996-02-13 2001-02-06 Zeneca Limited Quinazoline derivatives as VEGF inhibitors

Family Cites Families (34)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5369108A (en) * 1991-10-04 1994-11-29 Sloan-Kettering Institute For Cancer Research Potent inducers of terminal differentiation and methods of use thereof
US5747498A (en) * 1996-05-28 1998-05-05 Pfizer Inc. Alkynyl and azido-substituted 4-anilinoquinazolines
US6777217B1 (en) * 1996-03-26 2004-08-17 President And Fellows Of Harvard College Histone deacetylases, and uses related thereto
GB9718972D0 (en) * 1996-09-25 1997-11-12 Zeneca Ltd Chemical compounds
GB9800575D0 (en) 1998-01-12 1998-03-11 Glaxo Group Ltd Heterocyclic compounds
DE60037020T2 (de) 1999-07-09 2008-08-21 Glaxo Group Ltd., Greenford Anilinochinazoline als protein-tyrosin-kinasehemmer
UA74803C2 (uk) * 1999-11-11 2006-02-15 Осі Фармасьютікалз, Інк. Стійкий поліморф гідрохлориду n-(3-етинілфеніл)-6,7-біс(2-метоксіетокси)-4-хіназолінаміну, спосіб його одержання (варіанти) та фармацевтичне застосування
WO2001098277A2 (fr) 2000-06-22 2001-12-27 Pfizer Products Inc. Derives bicycliques substitues destines au traitement de la croissance cellulaire anormale
ATE340165T1 (de) 2001-02-26 2006-10-15 Univ Mcgill Kombi-moleküle, welche eine inhibierende wirkung auf die signalübertragung und dna-schädigende eigenschaften haben
US6562319B2 (en) * 2001-03-12 2003-05-13 Yissum Research Development Company Of The Hebrew University Of Jerusalem Radiolabeled irreversible inhibitors of epidermal growth factor receptor tyrosine kinase and their use in radioimaging and radiotherapy
IL164167A0 (en) * 2002-03-30 2005-12-18 Boehringer Ingelheim Pharma 4-(N-phenylamino)-quinazolines/ quinolines as tyrosine kinase inhibitors
JPWO2004018430A1 (ja) * 2002-08-23 2005-12-08 麒麟麦酒株式会社 ＴＧＦβ阻害活性を有する化合物およびそれを含んでなる医薬組成物
GB0309009D0 (en) 2003-04-22 2003-05-28 Astrazeneca Ab Quinazoline derivatives
JO2785B1 (en) 2003-05-27 2014-03-15 شركة جانسين فارماسوتيكا ان. في Quinazoline derivatives
EP1660479A1 (fr) * 2003-07-29 2006-05-31 Astrazeneca AB Derivees de piperidyl-quinazoline utilises comme inhibiteurs de la tyrosine kinase
JP4795952B2 (ja) 2003-09-16 2011-10-19 アストラゼネカ アクチボラグ チロシンキナーゼ阻害剤としてのキナゾリン誘導体
MXPA06003341A (es) * 2003-09-25 2006-06-08 Astrazeneca Ab Derivados de quinazolina.
WO2005097134A2 (fr) * 2004-03-31 2005-10-20 The Scripps Research Institute Inhibiteurs de proteine kinase a base de quinazoline
EP1745022B1 (fr) 2004-04-05 2014-08-13 Aton Pharma, Inc. Promedicaments sous forme d'inhibiteurs d'histones desacetylases
KR100735639B1 (ko) * 2004-12-29 2007-07-04 한미약품 주식회사 암세포 성장 억제 효과를 갖는 퀴나졸린 유도체 및 이의제조방법
NZ599464A (en) 2005-02-03 2014-03-28 Topotarget Uk Ltd Combination therapies using hdac inhibitors
BRPI0606905B1 (pt) * 2005-02-23 2021-06-01 Shionogi & Co., Ltd. Derivados de quinazolina tendo atividade inibitória de tirosina cinase e composição farmacêutica que os compreende
KR100832593B1 (ko) * 2005-11-08 2008-05-27 한미약품 주식회사 신호전달 저해제로서의 퀴나졸린 유도체 및 이의 제조방법
BR122018075851B1 (pt) * 2005-11-15 2022-01-11 Array Biopharma Inc Compostos relacionados ao tratamento de doença hiperproliferativa e processos para preparar compostos
WO2007131364A1 (fr) 2006-05-16 2007-11-22 Mcgill University Molécules hybrides ayant des propriétés mixtes d'agonisme du récepteur de la vitamine d et inhibitrice de l'histone désacétylase
AU2007288204A1 (en) 2006-08-22 2008-02-28 Concert Pharmaceuticals Inc. 4-aminoquinazoline derivatives and methods of use thereof
EP2061469B8 (fr) * 2006-09-11 2014-02-26 Curis, Inc. Inhibiteurs d'egfr à base de quinazoline
SG174772A1 (en) * 2006-09-11 2011-10-28 Curis Inc Multi-functional small molecules as anti-proliferative agents
KR101434164B1 (ko) 2006-09-11 2014-08-26 쿠리스 인코퍼레이션 아연 결합 부분을 함유한 퀴나졸린 계열 ｅｇｆｒ 억제제
US7547781B2 (en) * 2006-09-11 2009-06-16 Curis, Inc. Quinazoline based EGFR inhibitors containing a zinc binding moiety
CA2822776A1 (fr) 2006-10-28 2008-05-08 Methylgene Inc. Inhibiteurs de l'histone desacetylase
TWI377944B (en) 2007-06-05 2012-12-01 Hanmi Holdings Co Ltd Novel amide derivative for inhibiting the growth of cancer cells
US8119616B2 (en) 2007-09-10 2012-02-21 Curis, Inc. Formulation of quinazoline based EGFR inhibitors containing a zinc binding moiety
ES2526718T3 (es) 2007-09-10 2015-01-14 Curis, Inc. Inhibidores de EGFR basados en sales de tartrato o complejos de quinazolina que contienen un resto que se une al cinc

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5616582A (en) * 1992-01-20 1997-04-01 Zeneca Limited Quinazoline derivatives as anti-proliferative agents
US5942514A (en) * 1995-04-27 1999-08-24 Zeneca Limited Quinazoline derivatives
US6184225B1 (en) * 1996-02-13 2001-02-06 Zeneca Limited Quinazoline derivatives as VEGF inhibitors

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9434994B2 (en) 2004-05-27 2016-09-06 The Regents Of The University Of Colorado, A Body Corporate Methods for prediction of clinical outcome to epidermal growth factor receptor inhibitors by non-small cell lung cancer patients
US8735409B2 (en) 2009-12-21 2014-05-27 Qiang Zhang Quinazoline derivatives
US11524956B2 (en) 2011-03-04 2022-12-13 Newgen Therapeutics, Inc. Alkyne substituted quinazoline compound and methods of use

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JP2010502744A (ja) 2010-01-28
JP5580592B2 (ja) 2014-08-27
TWI399204B (zh) 2013-06-21
SG174774A1 (en) 2011-10-28
KR20090067169A (ko) 2009-06-24
BRPI0715016A2 (pt) 2013-05-28
KR101434164B1 (ko) 2014-08-26
CN101535279B (zh) 2015-05-20
IL197451A (en) 2015-08-31
AU2007296746B2 (en) 2012-07-05
CA2662617C (fr) 2014-11-18
US20080194578A1 (en) 2008-08-14
US20140005391A1 (en) 2014-01-02
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US20150284340A1 (en) 2015-10-08
KR20130028970A (ko) 2013-03-20
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US9024024B2 (en) 2015-05-05
IL197451A0 (en) 2009-12-24
US20140221403A1 (en) 2014-08-07
US8604044B2 (en) 2013-12-10
US8349856B2 (en) 2013-01-08
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AU2007296746A1 (en) 2008-03-20
TW200829249A (en) 2008-07-16
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